Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2824215 | 21 | 17063088 | intergenic variant | A/C | snv | 0.34 | 1 | ||||
rs773632957 | 19 | 45368650 | missense variant | T/G | snv | 1 | |||||
rs983889 | 5 | 15555377 | intron variant | G/T | snv | 0.55 | 1 | ||||
rs774690269 | 3 | 14178562 | missense variant | G/A;C | snv | 1.2E-05 | 1 | ||||
rs1383997 | 8 | 72005483 | intron variant | T/C | snv | 0.58 | 1 | ||||
rs150547487 | 16 | 3597425 | missense variant | T/C | snv | 9.9E-04 | 4.1E-03 | 1 | |||
rs1431381385 | 3 | 14167204 | missense variant | G/A | snv | 4.1E-06 | 1.4E-05 | 1 | |||
rs1486253194 | 3 | 14146063 | frameshift variant | CCAGTATCCTGGCC/- | del | 7.0E-06 | 1 | ||||
rs770726832 | 3 | 14170483 | missense variant | T/G | snv | 5.2E-05 | 1 | ||||
rs749251734 | 3 | 14147981 | frameshift variant | GACGATGTATCCA/- | delins | 1 | |||||
rs773629528 | 3 | 14178554 | synonymous variant | G/A;C | snv | 1.2E-05 | 7.0E-06 | 1 | |||
rs1395746092 | 19 | 43575449 | missense variant | T/C | snv | 7.0E-06 | 1 | ||||
rs1372047743 | 8 | 47960120 | missense variant | C/T | snv | 9.7E-06 | 3 | ||||
rs3087468 | 16 | 2040233 | missense variant | C/A | snv | 3 | |||||
rs1131691041 | 17 | 7676271 | frameshift variant | -/A | delins | 3 | |||||
rs1024708183 | 0.925 | 0.040 | 19 | 7909761 | missense variant | A/G | snv | 4 | |||
rs121965059 | 0.925 | 0.080 | 10 | 124403892 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 4 | |
rs1470755915 | 0.776 | 0.240 | 8 | 92005229 | missense variant | C/A | snv | 7.0E-06 | 10 | ||
rs927698341 | 0.776 | 0.240 | 8 | 92005280 | synonymous variant | C/A | snv | 4.0E-06 | 2.8E-05 | 10 | |
rs61748181 | 0.827 | 0.120 | 5 | 1294051 | missense variant | C/T | snv | 2.2E-02 | 2.2E-02 | 10 | |
rs863225281 | 0.776 | 0.200 | 2 | 29220829 | missense variant | G/C;T | snv | 12 | |||
rs281864719 | 0.763 | 0.240 | 2 | 29220831 | missense variant | A/C;G;T | snv | 14 | |||
rs2232365 | 0.716 | 0.480 | X | 49259429 | intron variant | T/C | snv | 16 | |||
rs1057520007 | 0.701 | 0.440 | 17 | 7674917 | missense variant | T/A;C;G | snv | 21 | |||
rs61754966 | 0.701 | 0.280 | 8 | 89978293 | missense variant | T/C;G | snv | 1.2E-03 | 23 |